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- Tasks: Join us as a QA Associate, ensuring compliance and quality in pharmaceutical operations.
- Company: Be part of a leading pharmaceutical company dedicated to excellence and innovation.
- Benefits: Enjoy a 9-month contract with opportunities for growth and skill development.
- Why this job: Make a real impact on product quality while collaborating with diverse teams.
- Qualifications: Strong GMP knowledge and attention to detail are essential; prior experience is a plus.
- Other info: This role offers a chance to mentor others and promote best practices.
The predicted salary is between 36000 - 60000 £ per year.
We are currently looking for a QA Associate to join a leading pharmaceutical company on a 9 month contract.
Key Responsibilities:
- Quality & Compliance Support: Monitor and assess site operations for compliance with GMP and internal procedures, identifying and escalating non-conformances through appropriate QMS channels.
- Documentation Review: Perform detailed, real-time review of manufacturing and laboratory documentation, ensuring accuracy, completeness, and adherence to regulatory standards.
- Continuous Improvement & Audit Readiness: Contribute to a state of audit readiness by actively participating in quality system improvements and continuous improvement initiatives.
- Compliance Issue Management: Utilize in-depth GMP and QMS knowledge to manage and escalate major and critical quality issues, including deviations and CAPAs.
- Cross-Functional Collaboration: Serve as a quality liaison for key stakeholders across manufacturing, technical operations, and supply chain teams.
- Training & Best Practice Promotion: Mentor team members on cGMP principles and best documentation practices, supporting a culture of compliance and proactive quality.
Required Skills & Competencies:
- Strong knowledge of GMP and pharmaceutical quality systems
- Proficient in documentation review and risk-based decision making
- High attention to detail with accurate data entry skills
- Strong communication and interpersonal skills
- Excellent organizational, planning, and time-management abilities
- IT literate (MS Office; familiarity with databases)
Preferred Experience:
- Prior experience in a GMP-regulated environment
- Working knowledge of deviations, CAPAs, and quality investigations
- Involvement in continuous improvement or pharmaceutical quality system (PQS) enhancement projects
Quality Assurance Associate employer: BioTalent
Contact Detail:
BioTalent Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Associate
✨Tip Number 1
Familiarise yourself with the latest GMP guidelines and regulations. This will not only help you understand the compliance landscape but also demonstrate your commitment to quality assurance during interviews.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those working in quality assurance roles. Attend relevant webinars or local meetups to gain insights and potentially get referrals for the position.
✨Tip Number 3
Prepare to discuss specific examples of how you've contributed to quality improvements or handled compliance issues in past roles. This will showcase your practical experience and problem-solving skills.
✨Tip Number 4
Research the company’s recent projects or initiatives related to quality assurance. Being knowledgeable about their work can help you tailor your conversation and show genuine interest during the interview process.
We think you need these skills to ace Quality Assurance Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience and skills relevant to the Quality Assurance role. Emphasise your knowledge of GMP, documentation review, and any previous work in a GMP-regulated environment.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for quality assurance in the pharmaceutical industry. Mention specific experiences where you contributed to compliance or continuous improvement initiatives.
Highlight Relevant Skills: In your application, clearly outline your strong communication, organisational, and time-management skills. Provide examples of how you've used these skills in past roles, especially in relation to quality systems.
Showcase Continuous Improvement Experience: If you have been involved in any continuous improvement projects or quality system enhancements, make sure to include this in your application. Detail your role and the impact of your contributions.
How to prepare for a job interview at BioTalent
✨Showcase Your GMP Knowledge
Make sure to highlight your understanding of Good Manufacturing Practices (GMP) during the interview. Be prepared to discuss specific examples from your past experience where you ensured compliance and how you handled any non-conformances.
✨Demonstrate Attention to Detail
Since this role requires a high level of accuracy, be ready to provide examples of how you've maintained meticulous documentation in previous positions. You might even want to bring a sample of your work to demonstrate your thoroughness.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills, especially regarding compliance issues and CAPAs. Think of scenarios where you successfully managed quality issues and be ready to explain your thought process and actions taken.
✨Emphasise Collaboration Skills
This position involves working with various teams, so be prepared to discuss how you've effectively collaborated with cross-functional teams in the past. Share specific instances where your communication skills helped resolve issues or improve processes.
